CFAP418 (NM_177965) Human Recombinant Protein
CAT#: TP761071
Purified recombinant protein of Human chromosome 8 open reading frame 37 (C8orf37), full length, with N-terminal HIS tag, expressed in E. coli, 50ug
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CNY 2,040.00
货期*
现货
规格
Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
A DNA sequence encoding human full-length C8orf37
|
Tag | N-His |
Predicted MW | 23.2 kDa |
Concentration | >0.05 µg/µL as determined by microplate BCA method |
Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Buffer | 25 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1% sarkosyl, 10% glycerol |
Note | For testing in cell culture applications, please filter before use. Note that you may experience some loss of protein during the filtration process. |
Storage | Store at -80°C. |
Stability | Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Reference Data | |
RefSeq | NP_808880 |
Locus ID | 157657 |
UniProt ID | Q96NL8 |
Refseq Size | 2254 |
Cytogenetics | 8q22.1 |
Refseq ORF | 621 |
Synonyms | BBS21; C8orf37; CORD16; FAP418; MOT25; RP64; smalltalk |
Summary | This gene encodes a ubiquitously expressed protein of unknown function. It has high levels of mRNA expression in the brain, heart, and retina and the protein co-localizes with polyglutamylated tubulin at the base of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have been associated with autosomal recessive cone-rod dystrophy (arCRD) and retinitis pigmentosa (arRP). [provided by RefSeq, Mar 2012] |
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